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组胺诱导的环磷酸腺苷变化与豚鼠回肠和兔肠系膜动脉平滑肌制剂机械活性之间的关系。

Relationship between histamine-induced changes of cyclic AMP and mechanical activity on smooth muscle preparations of the guinea-pig ileum and the rabbit mesenteric artery.

作者信息

Reinhardt D, Ritter E, Butzheinen R, Schümann H J

出版信息

Agents Actions. 1979 Jun;9(2):155-62. doi: 10.1007/BF02024727.

Abstract

On guinea-pig ileum and rabbit mesenteric artery contracted by high potassium (100 mM) histamine produced relaxations which were inhibited by the H2-receptor antagonist metiamide. These results are thus indicative for the role of H2-receptors in mediating relaxation and for H1-receptors in mediating contraction on smooth muscle. Time course studies for the relaxing and cyclic AMP responses to histamine showed that the cyclic AMP increase preceded the H2-receptor mediated relaxation. The cyclic AMP increase in response to histamine was prevented by metiamide, but remained unaffected by mepyramine on both the guinea-pig ileum and the rabbit mesenteric artery. In addition, dose-response curves obtained on the mesenteric artery demonstrated that the H2-receptor mediated depressor responses coincided with cyclic AMP increases. Thus, these results gave clear-cut evidence that cyclic AMP is an intracellular metabolic event only implicit in the H2-receptor mediated relaxation, but not in the H1-receptor mediated contraction on smooth muscle preparations.

摘要

在由高钾(100 mM)收缩的豚鼠回肠和兔肠系膜动脉上,组胺可产生舒张作用,该作用被H2受体拮抗剂甲硫米特抑制。因此,这些结果表明H2受体在介导平滑肌舒张中起作用,而H1受体在介导平滑肌收缩中起作用。对组胺舒张反应和环磷酸腺苷(cAMP)反应的时程研究表明,cAMP增加先于H2受体介导的舒张。甲硫米特可阻止组胺引起的cAMP增加,但在豚鼠回肠和兔肠系膜动脉上,美吡拉敏对其均无影响。此外,在肠系膜动脉上获得的剂量反应曲线表明,H2受体介导的降压反应与cAMP增加一致。因此,这些结果提供了明确的证据,即cAMP是一种仅与H2受体介导的平滑肌舒张有关的细胞内代谢事件,而与H1受体介导的平滑肌收缩无关。

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